da Silva Costa SM - Search Results

1

Association of HTRA1 rs11200638 with age-related macular degeneration (AMD) in Brazilian patients.

Lana TP, da Silva Costa SM, Ananina G, Hirata FE, Rim PHH, Medina FM, de Vasconcellos JPC, de Melo MB. Lana TP, et al. Among authors: da silva costa sm. Ophthalmic Genet. 2018 Jan-Feb;39(1):46-50. doi: 10.1080/13816810.2017.1354382. Epub 2017 Aug 28. Ophthalmic Genet. 2018. PMID: 28846052

2

Ménière's Disease: Molecular Analysis of Aquaporins 2, 3 and Potassium Channel KCNE1 Genes in Brazilian Patients.

Lopes Kde C, Sartorato EL, da Silva-Costa SM, de Macedo Adamov NS, Ganança FF. Lopes Kde C, et al. Among authors: da silva costa sm. Otol Neurotol. 2016 Sep;37(8):1117-21. doi: 10.1097/MAO.0000000000001136. Otol Neurotol. 2016. PMID: 27509294

3

Whole-exome sequencing indicates FLG2 variant associated with leg ulcers in Brazilian sickle cell anemia patients.

de Carvalho-Siqueira GQ, Ananina G, de Souza BB, Borges MG, Ito MT, da Silva-Costa SM, de Farias Domingos I, Falcão DA, Lopes-Cendes I, Bezerra MAC, da Silva Araújo A, Lucena-Araújo AR, de Souza Gonçalves M, Saad STO, Costa FF, de Melo MB. de Carvalho-Siqueira GQ, et al. Among authors: da silva costa sm. Exp Biol Med (Maywood). 2019 Aug;244(11):932-939. doi: 10.1177/1535370219849592. Epub 2019 May 12. Exp Biol Med (Maywood). 2019. PMID: 31079484 Free PMC article.

4

Epigenetic analysis in placentas from sickle cell disease patients reveals a hypermethylation profile.

Gil GP, Ananina G, Maschietto M, Lima SCS, da Silva Costa SM, Baptista LC, Ito MT, Costa FF, Costa ML, de Melo MB. Gil GP, et al. Among authors: da silva costa sm. PLoS One. 2022 Sep 21;17(9):e0274762. doi: 10.1371/journal.pone.0274762. eCollection 2022. PLoS One. 2022. PMID: 36129958 Free PMC article.

5

Single nucleotide polymorphisms of the GJB2 and GJB6 genes are associated with autosomal recessive nonsyndromic hearing loss.

Grillo AP, de Oliveira FM, de Carvalho GQ, Medrano RF, da Silva-Costa SM, Sartorato EL, de Oliveira CA. Grillo AP, et al. Among authors: da silva costa sm. Biomed Res Int. 2015;2015:318727. doi: 10.1155/2015/318727. Epub 2015 May 17. Biomed Res Int. 2015. PMID: 26075227 Free PMC article. Clinical Trial.

6

Analysis of mitochondrial alterations in Brazilian patients with sensorineural hearing loss using MALDI-TOF mass spectrometry.

Alves RM, da Silva Costa SM, do Amôr Divino Miranda PM, Ramos PZ, Marconi TG, Santos Oliveira G, Castilho AM, Sartorato EL. Alves RM, et al. Among authors: da silva costa sm. BMC Med Genet. 2016 May 26;17(1):41. doi: 10.1186/s12881-016-0303-5. BMC Med Genet. 2016. PMID: 27230773 Free PMC article.

7

Screening for the GJB2 c.-3170 G>A (IVS 1+1 G>A) mutation in Brazilian deaf individuals using multiplex ligation-dependent probe amplification.

da Silva-Costa SM, Coeli FB, Lincoln-de-Carvalho CR, Marques-de-Faria AP, Kurc M, Pereira T, Pomilio MC, Sartorato EL. da Silva-Costa SM, et al. Genet Test Mol Biomarkers. 2009 Oct;13(5):701-4. doi: 10.1089/gtmb.2009.0025. Genet Test Mol Biomarkers. 2009. PMID: 19715470

8

Angiogenesis-Related Genes in Endothelial Progenitor Cells May Be Involved in Sickle Cell Stroke.

Ito MT, da Silva Costa SM, Baptista LC, Carvalho-Siqueira GQ, Albuquerque DM, Rios VM, Ospina-Prieto S, Saez RC, Vieira KP, Cendes F, Ozelo MC, Saad STO, Costa FF, Melo MB. Ito MT, et al. Among authors: da silva costa sm. J Am Heart Assoc. 2020 Feb 4;9(3):e014143. doi: 10.1161/JAHA.119.014143. Epub 2020 Feb 3. J Am Heart Assoc. 2020. PMID: 32009522 Free PMC article.

9

A novel DFNB1 deletion allele supports the existence of a distant cis-regulatory region that controls GJB2 and GJB6 expression.

Wilch E, Azaiez H, Fisher RA, Elfenbein J, Murgia A, Birkenhäger R, Bolz H, Da Silva-Costa SM, Del Castillo I, Haaf T, Hoefsloot L, Kremer H, Kubisch C, Le Marechal C, Pandya A, Sartorato EL, Schneider E, Van Camp G, Wuyts W, Smith RJ, Friderici KH. Wilch E, et al. Among authors: da silva costa sm. Clin Genet. 2010 Sep;78(3):267-74. doi: 10.1111/j.1399-0004.2010.01387.x. Epub 2010 Mar 1. Clin Genet. 2010. PMID: 20236118 Free PMC article.

10

Newborn hearing screening and genetic testing in 8974 Brazilian neonates.

Nivoloni Kde A, da Silva-Costa SM, Pomílio MC, Pereira T, Lopes Kde C, de Moraes VC, Alexandrino F, de Oliveira CA, Sartorato EL. Nivoloni Kde A, et al. Among authors: da silva costa sm. Int J Pediatr Otorhinolaryngol. 2010 Aug;74(8):926-9. doi: 10.1016/j.ijporl.2010.05.015. Epub 2010 Jun 9. Int J Pediatr Otorhinolaryngol. 2010. PMID: 20538352

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

17 results

Search Page

Filters